Comparative Study Between (FC-SEMS) and (PC-SEMS) in the Palliation of Dysphagia Due to Malignant Neoplasm of Esophagus.

Sponsor
Instituto do Cancer do Estado de São Paulo (Other)
Overall Status
Recruiting
CT.gov ID
NCT06070376
Collaborator
(none)
34
1
2
11.5
3

Study Details

Study Description

Brief Summary

Esophageal cancer is the seventh most common type of cancer in the world, with an estimated global incidence of 604,100 new cases per year. The main symptom of esophageal cancer is dysphagia, associated or not with weight loss. Unfortunately, due to asymptomatic presentation in the early stages, more than half of patients are diagnosed in advanced stages of the disease, becoming ineligible for treatment with curative intent. In this sense, chemotherapy and radiotherapy are the pillars of palliative treatment, often regressing the injury and improving symptoms. However, some patients persist with dysphagia. In this scenario, esophageal prostheses are one of the main tools in the palliative treatment of esophageal cancer dysphagia, obtaining rapid and lasting relief of dysphagia. This study aims to compare fully covered (FC-SEMS) and partially covered (PC-SEMS) esophageal prostheses in this context, evaluating the number of reinterventions in each group, as well as the occurrence of adverse events. However, it is expected that with the data obtained it is possible to develop clearer and more effective protocols in the palliation of malignant dysphagia of esophageal stenosis.

Condition or Disease Intervention/Treatment Phase
  • Device: Fully Covered Esophageal Prosthesis (FC-SEMS)
  • Device: Partially Covered Esophageal Prosthesis (PC-SEMS)
N/A

Detailed Description

STUDY DESIGN: Prospective and randomized study will be conducted.

PREPARATION AND TECHNICAL STEPS OF THE PROCEDURE: The placement of the esophageal prosthesis will be performed under sedation or general anesthesia supervised by the anesthesiologist at the endoscopy service of the Cancer Institute of the State of São Paulo (ICESP). The tests will be performed under radioscopic control. The tests will be performed on an outpatient basis, and hospitalization may occur in case of clinical need.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
34 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Double (Participant, Investigator)
Primary Purpose:
Treatment
Official Title:
Comparative Study Between Fully Covered Esophageal Prosthesis (FC-SEMS) and Partially Covered Esophageal Prosthesis (PC-SEMS) in the Palliation of Dysphagia Due to Malignant Neoplasm of Esophagus.
Actual Study Start Date :
Jun 26, 2023
Anticipated Primary Completion Date :
Dec 20, 2023
Anticipated Study Completion Date :
Jun 10, 2024

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Group A

placement of the esophageal prostheses fully covered in the palliative treatment of malignant esophageal obstructions.

Device: Fully Covered Esophageal Prosthesis (FC-SEMS)
The placement of the Fully Covered Esophageal Prosthesis (FC-SEMS) will be performed under sedation or general anesthesia supervised by the anesthesiologist at the endoscopy service of the Cancer Institute of the State of São Paulo (ICESP). The tests will be performed under radioscopic control. The tests will be performed on an outpatient basis, and hospitalization may occur in case of clinical need.

Active Comparator: Group B

placement of the partially covered esophageal prostheses in the palliative treatment of malignant esophageal obstructions.

Device: Partially Covered Esophageal Prosthesis (PC-SEMS)
The placement of the Partially Covered Esophageal Prosthesis (PC-SEMS) will be performed under sedation or general anesthesia supervised by the anesthesiologist at the endoscopy service of the Cancer Institute of the State of São Paulo (ICESP). The tests will be performed under radioscopic control. The tests will be performed on an outpatient basis, and hospitalization may occur in case of clinical need.

Outcome Measures

Primary Outcome Measures

  1. Reinterventions [2 years]

    Number of reinterventions after the procedure.

Secondary Outcome Measures

  1. Adverse events and patency time of the prostheses [2 years]

    Number of adverse events

  2. Patency time of the prostheses. [2 years]

    Days without need a new prothesis or procedure

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Patients with advanced malignant neoplasm of the esophagus, whether or not undergoing chemotherapy or radiotherapy;

  • Dysphagia score greater than 2 or presence of malignant esophagorespiratory fistula;

  • Indication of palliation of dysphagia through the placement of esophageal prostheses in a multidisciplinary meeting.

Exclusion Criteria:
  • Patients under 18 years;

  • Extraesophageal neoplasms;

  • Lesions with longitudinal extension less than 30 mm;

  • Previous treatment with esophageal prosthesis;

  • Tumors easily transposed to standard endoscope (9.8mm).

Contacts and Locations

Locations

Site City State Country Postal Code
1 Instituto do Câncer do Estado de São Paulo São Paulo Brazil 01246-000

Sponsors and Collaborators

  • Instituto do Cancer do Estado de São Paulo

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Fauze Maluf Filho, MD, PhD, FASGE, Instituto do Cancer do Estado de São Paulo
ClinicalTrials.gov Identifier:
NCT06070376
Other Study ID Numbers:
  • NP3080/22
First Posted:
Oct 6, 2023
Last Update Posted:
Oct 6, 2023
Last Verified:
Oct 1, 2023
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Fauze Maluf Filho, MD, PhD, FASGE, Instituto do Cancer do Estado de São Paulo
Additional relevant MeSH terms:

Study Results

No Results Posted as of Oct 6, 2023